A citation-based method for searching scientific literature

Stephanie A Cohen, Shanna L Gustafson, Monica L Marvin, Bronson D Riley, Wendy R Uhlmann, S Bonnie Liebers, Julie A Rousseau. J Genet Couns 2012
Times Cited: 45







List of co-cited articles
202 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Preferences for in-person disclosure: Patients declining telephone disclosure characteristics and outcomes in the multicenter Communication Of GENetic Test Results by Telephone study.
Nina Beri, Linda J Patrick-Miller, Brian L Egleston, Michael J Hall, Susan M Domchek, Mary B Daly, Pamela Ganschow, Generosa Grana, Olufunmilayo I Olopade, Dominique Fetzer,[...]. Clin Genet 2019
8
25


Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.
Jean-Charles Lambert, Simon Heath, Gael Even, Dominique Campion, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, Diana Zelenika, Maria J Bullido, Béatrice Tavernier,[...]. Nat Genet 2009
2



Public attitudes about genetic testing for Alzheimer's disease.
P J Neumann, J K Hammitt, C Mueller, H M Fillit, J Hill, N A Tetteh, K S Kosik. Health Aff (Millwood) 2001
68
2




Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews carrying the E200K mutation in the prion protein gene.
S Spudich, J A Mastrianni, M Wrensch, R Gabizon, Z Meiner, I Kahana, H Rosenmann, E Kahana, S B Prusiner. Mol Med 1995
64
2


Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience.
Kurt D Christensen, J Scott Roberts, Charmaine D M Royal, Grace-Ann Fasaye, Thomas Obisesan, L Adrienne Cupples, Peter J Whitehouse, Melissa Barber Butson, Erin Linnenbringer, Norman R Relkin,[...]. Genet Med 2008
31
3

Genetic susceptibility testing versus family history-based risk assessment: Impact on perceived risk of Alzheimer disease.
Susan LaRusse, J Scott Roberts, Theresa M Marteau, Heather Katzen, Erin L Linnenbringer, Melissa Barber, Peter Whitehouse, Kimberly Quaid, Tamsen Brown, Robert C Green,[...]. Genet Med 2005
39
2


Health behavior changes after genetic risk assessment for Alzheimer disease: The REVEAL Study.
Serena Chao, J Scott Roberts, Theresa M Marteau, Rebecca Silliman, L Adrienne Cupples, Robert C Green. Alzheimer Dis Assoc Disord 2008
152
2

Letting the genome out of the bottle--will we get our wish?
David J Hunter, Muin J Khoury, Jeffrey M Drazen. N Engl J Med 2008
258
2


The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
213
2

How can we help people make sense of medical data?
S Woloshin, L M Schwartz. Eff Clin Pract 1999
26
3



Direct-to-consumer sales of genetic services on the Internet.
Sarah E Gollust, Benjamin S Wilfond, Sara Chandros Hull. Genet Med 2003
86
2

ASHG Statement* on direct-to-consumer genetic testing in the United States.
Kathy Hudson, Gail Javitt, Wylie Burke, Peter Byers. Obstet Gynecol 2007
85
2

Genetic risk and behavioural change.
T M Marteau, C Lerman. BMJ 2001
216
2


Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors.
Jill S Goldman, Susan E Hahn, Jennifer Williamson Catania, Susan LaRusse-Eckert, Melissa Barber Butson, Malia Rumbaugh, Michelle N Strecker, J Scott Roberts, Wylie Burke, Richard Mayeux,[...]. Genet Med 2011
162
2


Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
296
2

Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.
Lars Bertram, Matthew B McQueen, Kristina Mullin, Deborah Blacker, Rudolph E Tanzi. Nat Genet 2007
2

Genetics of Alzheimer's disease: a centennial review.
Nilüfer Ertekin-Taner. Neurol Clin 2007
147
2

The prion diseases.
J A Mastrianni, R P Roos. Semin Neurol 2000
24
4


Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
P Gambetti, P Parchi, R B Petersen, S G Chen, E Lugaresi. Brain Pathol 1995
150
2

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Elisa Majounie, Alan E Renton, Kin Mok, Elise G P Dopper, Adrian Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simon-Sanchez,[...]. Lancet Neurol 2012
732
2


Willingness-to-pay for predictive tests with no immediate treatment implications: a survey of US residents.
Peter J Neumann, Joshua T Cohen, James K Hammitt, Thomas W Concannon, Hannah R Auerbach, Chihui Fang, David M Kent. Health Econ 2012
80
2

Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.
C Klein, P P Pramstaller, B Kis, C C Page, M Kann, J Leung, H Woodward, C C Castellan, M Scherer, P Vieregge,[...]. Ann Neurol 2000
166
2

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium.
L A Farrer, L A Cupples, J L Haines, B Hyman, W A Kukull, R Mayeux, R H Myers, M A Pericak-Vance, N Risch, C M van Duijn. JAMA 1997
2

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
280
2


Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
Mariely DeJesus-Hernandez, Ian R Mackenzie, Bradley F Boeve, Adam L Boxer, Matt Baker, Nicola J Rutherford, Alexandra M Nicholson, NiCole A Finch, Heather Flynn, Jennifer Adamson,[...]. Neuron 2011
2

The prion diseases.
Khalilah Brown, James A Mastrianni. J Geriatr Psychiatry Neurol 2010
73
2

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
Chuong B Do, Joyce Y Tung, Elizabeth Dorfman, Amy K Kiefer, Emily M Drabant, Uta Francke, Joanna L Mountain, Samuel M Goldman, Caroline M Tanner, J William Langston,[...]. PLoS Genet 2011
352
2


Incidence of amyotrophic lateral sclerosis in Europe.
Giancarlo Logroscino, Bryan J Traynor, Orla Hardiman, Adriano Chiò, Douglas Mitchell, Robert J Swingler, Andrea Millul, Emma Benn, Ettore Beghi. J Neurol Neurosurg Psychiatry 2010
419
2


Genomics for the world.
Carlos D Bustamante, Esteban González Burchard, Francisco M De la Vega. Nature 2011
297
2


Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis.
Susan Byrne, Cathal Walsh, Catherine Lynch, Peter Bede, Marwa Elamin, Kevin Kenna, Russell McLaughlin, Orla Hardiman. J Neurol Neurosurg Psychiatry 2011
206
2



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.